Side effects and photosensitization of human tissues after aminolevulinic acid.

Aminolevulinic acid (ALA) is being used as a "prodrug" for photodynamic therapy. The side effects of ALA have been only anecdotally reported and these effects as well as pharmacokinetics of the photosensitizing end product of ALA, protoporphyrin IX (PpIX), in patients undergoing operation are unknown. This study systematically determines the side effects of ALA and pharmacokinetics of PpIX in patients undergoing abdominal surgery. Patients were given 30 or 60 mg/kg ALA preoperatively, kept in subdued light for 48 hr, and monitored clinically and with laboratory tests for 5 to 7 days and for at least 2 months thereafter. Periodic plasma samples and tissue biopsies were analyzed for PpIX concentrations using a photodiode array system. No patient developed symptoms of porphyria other than nausea and vomiting, which occurred in 20%. Nearly one-quarter of patients developed transient abnormal liver functions. No patient developed cutaneous phototoxicity, abnormal neurologic function, or unexpected postoperative laboratory tests. The times of peak plasma, skin, skeletal muscle, omental, mucosal, muscularis mucosal, and tumor concentrations of PpIX varied among patients. In general, PpIX concentrations were significantly greater with the higher dose of ALA. Tumor PpIX concentrations were significantly greater than in other tissues except liver. In conclusion, ALA, up to 60 mg/kg, is associated with minimal side effects in patients undergoing operation. Actual tissue concentrations of PpIX suggest that endogenous photosensitization using systemically administered ALA is a mode of PDT feasible for treatment of adenocarcinomas of the gastrointestinal tract in humans.

[1]  D. Kessel,et al.  Feasibility of photodynamic therapy using endogenous photosensitization for colon cancer. , 1996, Archives of surgery.

[2]  J Moan,et al.  DISTRIBUTION OF 5‐AMINOLEVULINIC ACID‐INDUCED PORPHYRINS IN NODULOULCERATIVE BASAL CELL CARCINOMA , 1995, Photochemistry and photobiology.

[3]  B. Henderson,et al.  PHOTOSENSITIZATION OF MURINE TUMOR, VASCULATURE and SKIN BY 5‐AMINOLEVULINIC ACID‐INDUCED PORPHYRIN , 1995, Photochemistry and photobiology.

[4]  T. Hasan,et al.  Biodistribution and phototoxicity of 5-aminolevulinic acid-induced PpIX in an orthotopic rat bladder tumor model. , 1995, The Journal of urology.

[5]  R. Lambert,et al.  Long-term survival after photodynamic therapy for esophageal cancer. , 1995, Gastroenterology.

[6]  A Gorchein,et al.  Photosensitisation and photodynamic therapy of oesophageal, duodenal, and colorectal tumours using 5 aminolaevulinic acid induced protoporphyrin IX--a pilot study. , 1995, Gut.

[7]  J. Kennedy,et al.  Using δ-Aminolevulinic Acid in Cancer Therapy , 1994 .

[8]  H. Kerl,et al.  Photodynamic therapy for mycosis fungoides after topical photosensitization with 5-aminolevulinic acid. , 1994, Journal of the American Academy of Dermatology.

[9]  I. Driver,et al.  Tumor vascular shutdown following photodynamic therapy based on polyhematoporphyrin or 5-aminolevulinic Acid. , 1994, International journal of oncology.

[10]  J. Reguła,et al.  Photodynamic therapy using 5-aminolaevulinic acid for experimental pancreatic cancer--prolonged animal survival. , 1994, British Journal of Cancer.

[11]  P. Speight,et al.  Photodynamic therapy of oral cancer: photosensitisation with systemic aminolaevulinic acid , 1993, The Lancet.

[12]  A. J. MacRobert,et al.  Oral versus intravenous administration of 5-aminolaevulinic acid for photodynamic therapy. , 1993, British Journal of Cancer.

[13]  S. Steinberg,et al.  Phase I study of debulking surgery and photodynamic therapy for disseminated intraperitoneal tumors. , 1993, International journal of radiation oncology, biology, physics.

[14]  J Moan,et al.  Distribution and photosensitizing efficiency of porphyrins induced by application of exogenous 5‐aminolevulinic acid in mice bearing mammary carcinoma , 1992, International journal of cancer.

[15]  S. G. Bown,et al.  Photodynamic therapy of the normal rat stomach: a comparative study between di-sulphonated aluminium phthalocyanine and 5-aminolaevulinic acid. , 1992, British Journal of Cancer.

[16]  R. van Hillegersberg,et al.  Selective accumulation of endogenously produced porphyrins in a liver metastasis model in rats. , 1992, Gastroenterology.

[17]  J C Kennedy,et al.  Endogenous protoporphyrin IX, a clinically useful photosensitizer for photodynamic therapy. , 1992, Journal of photochemistry and photobiology. B, Biology.

[18]  D. Phillips,et al.  Fluorescence distribution and photodynamic effect of ALA-induced PP IX in the DMH rat colonic tumour model. , 1992, British Journal of Cancer.

[19]  M. M. el-Sharabasy,et al.  Porphyrin metabolism in some malignant diseases. , 1992, British Journal of Cancer.

[20]  N. Schoenfeld,et al.  The heme biosynthetic pathway in lymphocytes of patients with malignant lymphoproliferative disorders. , 1988, Cancer letters.

[21]  L. Leibovici,et al.  Activity of porphobilinogen deaminase in peripheral blood mononuclear cells of patients with metastatic cancer , 1988, Cancer.

[22]  E Glatstein,et al.  PROTECTION AGAINST DIHEMATOPORPHYRIN ETHER PHOTOSENSITIVITY , 1988, Photochemistry and photobiology.

[23]  H. Barr,et al.  Photodynamic therapy in the normal rat colon with phthalocyanine sensitisation. , 1987, British Journal of Cancer.

[24]  Thomas S. Mang,et al.  THE THEORY OF PHOTODYNAMIC THERAPY DOSIMETRY: CONSEQUENCES OF PHOTO‐DESTRUCTION OF SENSITIZER , 1987 .

[25]  William R. Potter,et al.  The Theory Of Photodynamic Therapy Dosimetry: Consequences Of Photodestruction Of Sensitizer , 1987, Other Conferences.

[26]  N. Schoenfeld,et al.  Increased porphobilinogen deaminase activity in patients with malignant lymphoproliferative diseases. A helpful diagnostic test. , 1987, JAMA.

[27]  W. Star,et al.  Destruction of rat mammary tumor and normal tissue microcirculation by hematoporphyrin derivative photoradiation observed in vivo in sandwich observation chambers. , 1986, Cancer research.

[28]  H. Dailey,et al.  Differential interaction of porphyrins used in photoradiation therapy with ferrochelatase. , 1984, The Biochemical journal.

[29]  M. Valsamis,et al.  Abnormal iron and water metabolism in acute intermittent porphyria with new morphologic findings. , 1972, The American journal of medicine.

[30]  A. Neuberger,et al.  The metabolism of δ-aminolaevulic acid. 1. Normal pathways, studied with the aid of 15N , 1956 .

[31]  D. Kessel,et al.  Photodynamic Therapy Using Endogenous Photosensitization for Gastrointestinal Tumors , 1997, The Yale Journal of Biology and Medicine.

[32]  E G Hahn,et al.  Photodynamic therapy: successful destruction of gastrointestinal cancer after oral administration of aminolevulinic acid. , 1995, Gastrointestinal Endoscopy.

[33]  H Kerl,et al.  Topical photodynamic therapy with endogenous porphyrins after application of 5-aminolevulinic acid. An alternative treatment modality for solar keratoses, superficial squamous cell carcinomas, and basal cell carcinomas? , 1993, Journal of the American Academy of Dermatology.

[34]  R. van Hillegersberg,et al.  Photodynamic therapy for gastrointestinal tumors. , 1991, Scandinavian journal of gastroenterology. Supplement.

[35]  N. Navone,et al.  Heme biosynthesis in human breast cancer--mimetic "in vitro" studies and some heme enzymic activity levels. , 1990, The International journal of biochemistry.